Not CRISPR data: the image illustrates antibody quality for visualizing CRISPR experiment results.
Not CRISPR data: the image illustrates antibody quality for visualizing CRISPR experiment results.
ACOT11 CRISPR Activation Plasmid (h): sc-406653-ACT
- Target species: human
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- ACOT11 CRISPR Activation Plasmid (h) is a synergistic activation mediator (SAM) transcription activation system designed to specifically upregulate gene expression
- ACOT11 CRISPR Activation Plasmid (h) consists of three plasmids at a 1:1:1 mass ratio: a plasmid encoding the deactivated Cas9 (dCas9) nuclease (D10A and N863A) fused to the transactivation domain VP64, and a blasticidin resistance gene; a plasmid encoding the MS2-p65-HSF1 fusion protein, and a hygromycin resistance gene; a plasmid encoding a target-specific 20 nt guide RNA fused to two MS2 RNA aptamers, and a puromycin resistance gene
- The resulting SAM complex binds to a site-specific region approximately 200-250 nt upstream of the transcriptional start site and provides robust recruitment of transcription factors for highly efficient gene activation
- gRNAs encoded by ACOT11 CRISPR Activation Plasmid (h) and ACOT11 CRISPR Activation Plasmid (h2) target distinct regulatory regions upstream of the ACOT11 transcriptional start site. One or both designs may be available
- Following transfection, gene knockout efficiency can be assayed by WB, IF or IHC using antibody: ACOT11 Antibody (D-4): sc-398738
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
ACOT11 CRISPR Activation Plasmid (h) | sc-406653-ACT | 20 µg | $397.00 |
ACOT11 (acyl-CoA thioesterase 11) encodes a lipid metabolic enzyme that hydrolyzes long-chain acyl-CoA thioesters to free fatty acids and CoA, thereby tuning intracellular acyl-CoA pools. By modulating fatty acid utilization and lipid signaling intermediates, ACOT11 is linked to mitochondrial and peroxisomal lipid handling, energy homeostasis, and broader fatty acid oxidation and lipogenesis networks. Changes in acyl-CoA balance can influence oxidative stress responses and metabolic remodeling, processes frequently perturbed in obesity, insulin resistance, and fatty liver–associated pathways. Human ACOT11 is therefore a useful target for mechanistic studies of metabolic regulation and lipid-driven cellular phenotypes.
ACOT11 CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous ACOT11 expression without altering the underlying DNA sequence.
ACOT11 CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the ACOT11 locus in human cell lines. The system is built around a catalytically inactive Cas9 (dCas9) carrying two inactivating mutations (D10A and N863A) that eliminate nuclease activity while preserving DNA binding. This dCas9 is fused to VP64, a potent transcriptional activator, and is co-expressed with a blasticidin resistance gene for selection. The second plasmid encodes the MS2-p65-HSF1 fusion protein, a secondary activator complex that works in concert with dCas9-VP64, alongside a hygromycin resistance gene. The third plasmid encodes a target-specific 20 nt sgRNA fused to two MS2 RNA aptamers that recruit the MS2-p65-HSF1 complex to the activation site, accompanied by a puromycin resistance gene. The three plasmids are delivered at a 1:1:1 mass ratio for balanced expression of all system components.
Once assembled at the target locus, the SAM complex binds within approximately 200 bp upstream of the ACOT11 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous ACOT11 expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native ACOT11 locus and enabling the study of ACOT11-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of ACOT11 pathway restoration in tumor cells with silenced or reduced ACOT11 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.